microRNA 193a-5p Regulates Levels of Nucleolar- and Spindle-Associated Protein 1 to Suppress Hepatocarcinogenesis

Sanchari Roy, Guido J. Hooiveld, Marco Seehawer, Stefano Caruso, Florian Heinzmann, Anne T. Schneider, Anna K. Frank, David Vargas Cardenas, Roland Sonntag, Mark Luedde, Christian Trautwein, Ilan Stein, Eli Pikarsky, Sven Loosen, Frank Tacke, Marc Ringelhan, Seda Kilinc Avsaroglu, Andrei Goga, Marie Annick Buendia, Mihael VucurMathias Heikenwalder, Jessica Zucman-Rossi, Lars Zender, Christoph Roderburg, Tom Luedde*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

73 Scopus citations


Background & Aims: We performed an integrated analysis to identify microRNAs (miRNAs) and messenger RNAs (mRNAs) with altered expression in liver tumors from 3 mouse models of hepatocellular carcinoma (HCC) and human tumor tissues. Methods: We analyzed miRNA and mRNA expression profiles of liver tissues from mice with diethylnitrosamine-induced hepatocarcinogenesis, conditional expression of lymphotoxin alpha and lymphotoxin beta, or inducible expression of a Myc transgene (Tet-O-Myc mice), as well as male C57BL/6 mice (controls). miRNA mimics were expressed and miRNAs and mRNAs were knocked down in human (Huh7, Hep3B, JHH2) hepatoma cell lines; cells were analyzed for viability, proliferation, apoptosis, migration, and invasion. Cells were grown as xenograft tumors in nude mice and analyzed. We combined in silico target gene prediction with mRNA profiles from all 3 mouse models. We quantified miRNA levels in 146 fresh-frozen tissues from patients (125 HCCs, 17 matched nontumor tissues, and 4 liver samples from patients without cancer) and published human data sets and tested correlations with patient survival times using Kaplan-Meier curves and the log-rank test. Levels of NUSAP1 mRNA were quantified in 237 HCCs and 5 nontumor liver samples using the TaqMan assay. Results: Levels of the miRNA 193a-5p (MIR193A-5p) were reduced in liver tumors from all 3 mouse tumor models and in human HCC samples, compared with nontumor liver tissues. Expression of a MIR193A-5p mimic in hepatoma cells reduced proliferation, survival, migration, and invasion and their growth as xenograft tumors in nude mice. We found nucleolar and spindle-associated protein 1 (NUSAP1) to be a target of MIR193A-5p; HCC cells and tissues with low levels of MIR193A-5p had increased expression of NUSAP1. Increased levels of NUSAP1 in HCC samples correlated with shorter survival times of patients. Knockdown of NUSAP1 in Huh7 cells reduced proliferation, survival, migration, and growth as xenograft tumors in nude mice. Hydrodynamic tail-vein injections of a small hairpin RNA against NUSAP1 reduced growth of Akt1-Myc–induced tumors in mice. Conclusions: MIR193A-5p appears to prevent liver tumorigenesis by reducing levels of NUSAP1. Levels of MIR193A-5p are reduced in mouse and human HCC cells and tissues, leading to increased levels of NUSAP1, associated with shorter survival times of patients. Integrated analyses of miRNAs and mRNAs in tumors from mouse models can lead to identification of therapeutic targets in humans. The currently reported miRNA and mRNA profiling data have been submitted to the Gene Expression Omnibus (super-series accession number GSE102418).

Original languageAmerican English
Pages (from-to)1951-1966.e26
Issue number6
StatePublished - Dec 2018

Bibliographical note

Funding Information:
Funding Research in the laboratory of Tom Luedde is supported by a Mildred-Scheel Endowed Professorship from the German Cancer Aid (Deutsche Krebshilfe), the German Research Foundation (DFG) (LU 1360/3–1 and SFB-TRR57/P06), the Interdisciplinary Centre for Clinical Research (IZKF) Aachen, Germany, and the Ernst-Jung-Foundation, Hamburg. Moreover, this work was supported by project grants from the German Research Foundation (DFG RO 4317/4–1) and a START grant from the medical faculty RWTH Aachen to Christoph Roderburg. The group of Jessica Zucman-Rossi is supported by the Ligue Nationale contre le Cancer (Equipe Labellisée), Labex OncoImmunology (investissement d'avenir), Coup d'Elan de la Fondation Bettencourt-Shueller, the SIRIC CARPEM, and Fondation Mérieux. Mathias Heikenwalder was supported by the SFB179 and 209, an ERC consolidator grant (HepatoMetaboPath), and the European Union's Horizon 2020 research and innovation program under grant agreement No 667273. Andrei Goga was supported by National Institutes of Health R01CA170447 and U19CA179512.

Publisher Copyright:
© 2018 AGA Institute


  • Gene Regulation
  • Liver Cancer
  • Systems Biology
  • Translation


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